This brand name is authorized in Cyprus, France, Ireland, Malta, South Africa, Spain, UK.
The drug MAINTELYTE contains a combination of these active pharmaceutical ingredients (APIs):
1
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UNII
LX22YL083G - DEXTROSE MONOHYDRATE
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Glucose is frequently used in both adults and children to restore blood glucose concentrations in the treatment of hypoglycaemia resulting from insulin excess or from other causes. The metabolism of glucose is an energy source for the body. |
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2
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UNII
451W47IQ8X - SODIUM CHLORIDE
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Sodium chloride is the principle salt involved in maintaining the osmotic tension of blood and tissues. Changes in osmotic tension influence the movement of fluids and diffusion of salts in cellular tissue. |
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3
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UNII
4550K0SC9B - SODIUM ACETATE
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4
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UNII
660YQ98I10 - POTASSIUM CHLORIDE
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Potassium plays a vital physiological role in maintenance of normal electrical excitability of nerve and muscle. It is also important in the genesis and correction of imbalances of acid-base metabolism. |
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5
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UNII
02F3473H9O - MAGNESIUM CHLORIDE
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Below package inserts are available for further reading:
| Document | Type | Information Source | |
|---|---|---|---|
| MAINTELYTE Solution for infusion | MPI, EU: SmPC | Medicines & Healthcare Products Regulatory Agency (GB) |
This drug has been classified in the anatomical therapeutic chemical (ATC) classification system as follows:
| ATC Group | Classification | |
|---|---|---|
| B05BB02 | Electrolytes with carbohydrates | B Blood and blood forming organs → B05 Blood substitutes and perfusion solutions → B05B I.V. solutions → B05BB Solutions affecting the electrolyte balance |
This drug has been assigned below unique identifiers within the countries it is being marketed:
| Country | Identification scheme | Identifier(s) |
|---|---|---|
| ES | Centro de información online de medicamentos de la AEMPS | 84093 |
| FR | Base de données publique des médicaments | 67968730 |
| GB | Medicines & Healthcare Products Regulatory Agency | 379955 |
| MT | Medicines Authority | MA1277/01901 |
| ZA | Health Products Regulatory Authority | F/24/65, W/24/222 |
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